Canonical Allele Identifier: CA1868278355

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101424807_101424810delinsACAT , CM000671.2:g.101424807_101424810delinsACAT	GRCh38
NC_000009.11:g.104187089_104187092delinsACAT , CM000671.1:g.104187089_104187092delinsACAT	GRCh37
NC_000009.10:g.103226910_103226913delinsACAT	NCBI36
NG_012387.1:g.15971_15974delinsATGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.999+33_999+36delinsATGT MANE Select	ENSP00000497767.1:n.999+33_999+36delinsATGT
ENST00000648064.1:c.999+33_999+36delinsATGT	ENSP00000497990.1:n.999+33_999+36delinsATGT
ENST00000648758.1:c.999+33_999+36delinsATGT	ENSP00000497731.1:n.999+33_999+36delinsATGT
ENST00000649902.1:c.*3_*6delinsATGT	ENSP00000497216.1:n.*3_*6delinsATGT
ENST00000374855.8:c.999+33_999+36delinsATGT	ENSP00000363988.4:n.999+33_999+36delinsATGT
ENST00000616752.1:c.*11+33_*11+36delinsATGT	ENSP00000481363.1:n.*11+33_*11+36delinsATGT
NM_000035.3:c.999+33_999+36delinsATGT	NP_000026.2:n.999+33_999+36delinsATGT
NM_000035.4:c.999+33_999+36delinsATGT MANE Select	NP_000026.2:n.999+33_999+36delinsATGT